A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100664



Internal ID21279736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:652583..655916hg38UCSC Ensembl
Innerchr20:633227..636560hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383334
hg193334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112047
Supporting Variants
Samplessample289
Known GenesSRXN1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100664
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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